Service advice and planning
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Validation master plans
18 November 2025A validation master plan summarises all planned validation activities in a medicines preparation or manufacturing unit.
Use of PGDs by trainee registered healthcare professionals
12 February 2026Advice on the use of Patient Group Directions by registered healthcare professionals who are undertaking training and/or competency assessment
Understanding local governance in CTIMPs
12 December 2022Sponsor pharmacy's role in ensuring appropriate local governance arrangements for CTIMPs
Understanding iQAAPS
6 November 2025An introduction to the iQAAPS system, with information on how to access the system, find training resources and support contacts
Understanding essential documentation for clinical trials submissions
8 December 2022Sponsor responsibilities for writing and maintaining essential documents required for Clinical Trial Authorisation applications
Tissue engineered products
13 February 2026This document outlines key areas for focus of pharmaceutical expertise prior to an organisation implementing tissue engineered products.
The role of the sponsor pharmacy in clinical trials of investigational medicinal products (CTIMPs)
21 November 2024Identifying key areas where pharmaceutical expertise is required by sponsors for conducting non-commercial clinical trials
Supporting funding applications for CTIMPs
21 November 2024Sponsor pharmacy role in funding applications and establishing costs for sponsor activities
Supply and administration of medicines by staff group (P to Z)
29 July 2025Different staff groups have different permissions with respect to medicines supply and administration and it is important to ensure legislation is followed.
Supply and administration of medicines by staff group (H to O)
17 June 2025Different staff groups have different permissions with respect to medicines supply and administration and it is important to ensure legislation is followed.